机译:p.Ala546> Asp和p.Arg555>两个中国大的I型角膜营养不良大家族中TGFBI基因的Trp突变及其临床表现
Ping YuDepartment of Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, P. R. China.Yangshun GuDepartment of Ophthalmology, The First Affiliated Hospital, School of Medicine, Hangzhou, P. R. China.Fan JinDepartment of Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, P. R. China.Rongrong HuDepartment of Ophthalmology, The First Affiliated Hospital, School of Medicine, Hangzhou, P. R. China.Lili ChenDepartment of Ophthalmology, The First Affiliated Hospital, School of Medicine, Hangzhou, P. R. China.Xiaoyi YanDepartment of Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, P. R. China.Yuehong YangDepartment of Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, P. R. China.Ming QiDepartment of Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, P. R. China.Department of Ophthalmology, The First Affiliated Hospital, School of Medicine, Hangzhou, P. R. China.ZJU-Adinovo Center for Genetic & Genomic Medicine, James Watson Institute of Genome Sciences, Zhejiang University, Hangzhou, P. R. China.University of Rochester Medical Center, Rochester, New York.;
Granular Corneal Dystrophy Type;
机译:p.Ala546> Asp和p.Arg555>两个中国大型I型角膜营养不良家庭的TGFBI基因Trp突变及其临床表现
机译:TGFBI中典型的R555W突变引起的非典型性I型角膜营养不良的中国家庭
机译:TGFBI中典型的R555W突变引起的非典型性I型角膜营养不良的中国家庭
机译:一种简单的DNA芯片,用于诊断βigh3基因突变引起的最常见的角膜营销蛋白酶
机译:因子V Leiden和凝血酶原基因突变携带者临床表现的危险因素。
机译:TGFBI中典型的R555W突变引起的非典型性I型角膜营养不良的中国家庭
机译:TGFBI基因的自发突变引起的两种REIS-Bücklers角膜营养不良(III型)的两种情况